These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 20001581)

  • 1. Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization.
    Yu S; Kielt M; Stegner AL; Kibiryeva N; Bittel DC; Cooley LD
    Genet Test Mol Biomarkers; 2009 Dec; 13(6):751-60. PubMed ID: 20001581
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.
    Scott F; Murphy K; Carey L; Greville W; Mansfield N; Barahona P; Robertson R; McLennan A
    Ultrasound Obstet Gynecol; 2013 May; 41(5):500-7. PubMed ID: 23401365
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
    Boehm D; Herold S; Kuechler A; Liehr T; Laccone F
    Hum Mutat; 2004 Apr; 23(4):368-78. PubMed ID: 15024731
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A method for accurate detection of genomic microdeletions using real-time quantitative PCR.
    Weksberg R; Hughes S; Moldovan L; Bassett AS; Chow EW; Squire JA
    BMC Genomics; 2005 Dec; 6():180. PubMed ID: 16351727
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
    Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
    Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Validation of multiplex ligation-dependent probe amplification for confirmation of array comparative genomic hybridization.
    Jennings LJ; Yu M; Fitzpatrick C; Smith FA
    Diagn Mol Pathol; 2011 Sep; 20(3):166-74. PubMed ID: 21817904
    [TBL] [Abstract][Full Text] [Related]  

  • 7. ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.
    South ST; Lee C; Lamb AN; Higgins AW; Kearney HM;
    Genet Med; 2013 Nov; 15(11):901-9. PubMed ID: 24071793
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of real-time quantitative PCR as a standard cytogenetic diagnostic tool for confirmation of microarray (aCGH) results and determination of inheritance.
    Wang R; Carter J; Lench N
    Genet Test Mol Biomarkers; 2013 Nov; 17(11):821-5. PubMed ID: 24024523
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Quantitative PCR evaluation of deletions/duplications identified by array CGH.
    Baldan F; Passon N; Burra S; Demori E; Russo PD; Damante G
    Mol Cell Probes; 2019 Aug; 46():101421. PubMed ID: 31302230
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.
    Yu S; Bittel DC; Kibiryeva N; Zwick DL; Cooley LD
    Am J Clin Pathol; 2009 Sep; 132(3):349-60. PubMed ID: 19687311
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Quantitative PCR in the diagnosis of Leishmania].
    Mortarino M; Franceschi A; Mancianti F; Bazzocchi C; Genchi C; Bandi C
    Parassitologia; 2004 Jun; 46(1-2):163-7. PubMed ID: 15305709
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Application of DNA Microarray to Clinical Diagnostics.
    Patel A; Cheung SW
    Methods Mol Biol; 2016; 1368():111-32. PubMed ID: 26614072
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
    Chen CP; Chang SD; Su YN; Chen M; Chern SR; Su JW; Chen YT; Chen WL; Pan CW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocol.
    Wou K; Hyun Y; Chitayat D; Vlasschaert M; Chong K; Wasim S; Keating S; Shannon P; Kolomietz E
    Eur J Med Genet; 2016 Aug; 59(8):417-24. PubMed ID: 27233578
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Copy number variation in Fayoumi and Leghorn chickens analyzed using array comparative genomic hybridization.
    Abernathy J; Li X; Jia X; Chou W; Lamont SJ; Crooijmans R; Zhou H
    Anim Genet; 2014 Jun; 45(3):400-11. PubMed ID: 24628374
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comparison of the SYBR Green and the hybridization probe format for real-time PCR detection of HHV-6.
    Fernández F; Gutiérrez J; Sorlózano A; Romero JM; Soto MJ; Ruiz-Cabello F
    Microbiol Res; 2006; 161(2):158-63. PubMed ID: 16427520
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation.
    Hayes JL; Tzika A; Thygesen H; Berri S; Wood HM; Hewitt S; Pendlebury M; Coates A; Willoughby L; Watson CM; Rabbitts P; Roberts P; Taylor GR
    Genomics; 2013 Sep; 102(3):174-81. PubMed ID: 23598253
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia.
    Braude I; Vukovic B; Prasad M; Marrano P; Turley S; Barber D; Zielenska M; Squire JA
    BMC Genomics; 2006 Jun; 7():138. PubMed ID: 16756668
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A one-step prescreening for point mutations and large rearrangement in BRCA1 and BRCA2 genes using quantitative polymerase chain reaction and high-resolution melting curve analysis.
    Coulet F; Pires F; Rouleau E; Lefol C; Martin S; Colas C; Cohen-Haguenauer O; Giurgea I; Fajac A; Noguès C; Demange L; Hardouin A; Lidereau R; Soubrier F
    Genet Test Mol Biomarkers; 2010 Oct; 14(5):677-90. PubMed ID: 20858050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Application of chromosomal microarray in the evaluation of abnormal prenatal findings.
    Yatsenko SA; Davis S; Hendrix NW; Surti U; Emery S; Canavan T; Speer P; Hill L; Clemens M; Rajkovic A
    Clin Genet; 2013 Jul; 84(1):47-54. PubMed ID: 23020214
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.